Molecular Characterization of Cosenza Mutation among Patients with Glucose-6-Phosphate Dehydrogenase Deficiency in Khuzestan Province, Southwest Iran
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is one of the most common hereditary enzymatic disorders in human, increases the vulnerability of erythrocytes to oxidative stress. It is also characterized by remarkable molecular and biochemical heterogeneity. According to previous investigations...
محفوظ في:
| المؤلفون الرئيسيون: | , , , |
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| التنسيق: | Artigo |
| اللغة: | Inglês |
| منشور في: |
Shiraz University of Medical Sciences
2011-03-01
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| سلاسل: | Iranian Journal of Medical Sciences |
| الموضوعات: | |
| الوصول للمادة أونلاين: | http://ijms.sums.ac.ir/files/PDFfiles/08-Dr_%20Kazemi%20Nezhad.pdf |
| الوسوم: |
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